form
solution
Quality Level
usage
sufficient for ≥600 reactions
feature
PCR Additives
concentration
100 ×
technique(s)
PCR: suitable
color
red
input
crude DNA
solubility
water: soluble
storage temp.
2-8°C
General description
Sigma′s Reference Dye for quantitative polymerase chain reaction (qPCR) is a proprietary dye for use with real-time PCR. It is used for the normalization of reaction data when using SYBR Green, molecular probes, or dual-labeled probe chemistries for real-time detection. The Reference Dye is supplied as a 100× solution with a maximum excitation and emission of 586 nm and 605 nm, respectively. Instrument settings for ROX reference dye are satisfactory for the measurement of Reference Dye for qPCR.
Application
Reference Dye for Quantitative PCR has been used:
- in the preparation of mastermix for real time-quantitative polymerase chain reaction (RT-qPCR)
- as a component of the reaction mixture for detection of Clostridium difficile by quantitative polymerase chain reaction (qPCR)
- for analyzing the degree of cellular DNA contamination by qPCR
Other Notes
Reference Dye for Quantitative PCR is forR&D use only. Not for drug, household, or other uses.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
저장 등급
12 - Non Combustible Liquids
wgk
WGK 3
ppe
Eyeshields, Gloves
프로토콜
Protocol describes amplification of DNA through quantitative PCR with SYBR Green. Consistent batch-to-batch performance can be achieved with large numbers of PCR reactions.
Our SYBR Green qPCR Protocol is a method designed to detect accurate quantification of gene expression and RT-PCR reactions
SYBR Green qPCR 프로토콜은 유전자 발현 및 RT-PCR 반응의 정확한 정량화를 감지하도록 설계된 방법입니다.
문서
Identify causes and remedies for SDS-PAGE sample preparation challenges and optimize electrophoresis conditions.
Increased environmental sample area and recovery of Clostridium difficile spores from hospital surfaces by quantitative PCR and enrichment culture
Brown KA, et al.
Infection Control and Hospital Epidemiology : The Official Journal of the Society of Hospital Epidemiologists of America, 39(8), 917-923 (2018)
Partial deletion of rng (RNase G)-enhanced homoethanol fermentation of xylose by the non-transgenic Escherichia coli RM10
Manow R, et al.
Journal of Industrial Microbiology & Biotechnology, 39(7), 977-985 (2012)
Sambrook, J. et al.
Molecular Cloning: A Laboratory Manual, 3rd (2000)
국제 무역 품목 번호
| SKU | GTIN |
|---|---|
| R4526-.3ML | 04061836695354 |
| R4526-20RXN | 04061832933283 |
| R4526-5ML | 04061837693939 |

